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British Journal of Haematology|January 1, 1996
A novel mutation (Leu817Pro) causing type 2A von Willebrand diseaseD Gemmati, M L Serino, S Moratelli, et al.
Minerva Pediatrica|May 5, 2010
[Acute respiratory stridor in infancy]I Corsini, M Gallucci, E Di Palmo, et al.
Maturitas|December 22, 1999
GH, IGFBP-1, and IGFBP-3 response to oral glucose tolerance test in perimenopausal women: no influence of body mass indexF Bernardi, F Petraglia, M Seppälä, et al.
Pediatric Pulmonology|January 1, 1990
Bronchial reactivity and sex hormone: study in a Turner's populationM P Villa, F Bernardi, M Burnaccini, et al.
Journal of Endocrinological Investigation|June 13, 1998
Hypothalamic amenorrhea and cardiovascular hormones: changes of plasma calcitonin gene-related peptide and atrial natriuretic peptide levelsF Bernardi, A Valentini, A Margutti, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|August 31, 1984
Human leukemic K562 cells: differential effects of 5-azacytidine on DNA methylation of epsilon-, gamma-globin and 7SL RNA genesL del Senno, F Conconi, R Barbieri, et al.
Pediatric Pulmonology|November 1, 1986
Modification of nonspecific bronchial reactivity in hypothyroid children under different regimens of substitutive opotherapyM P Villa, G Cerimoniale, F Bernardi, et al.
Nucleic Acids Research|November 15, 1996
Identification of a (CUG)n triplet repeat RNA-binding protein and its expression in myotonic dystrophyL T Timchenko, J W Miller, N A Timchenko, et al.
The American Journal of Pathology|July 11, 2009
Expression of RNA CCUG repeats dysregulates translation and degradation of proteins in myotonic dystrophy 2 patientsElizabeth Salisbury, Benedikt Schoser, Christiane Schneider-Gold, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 31, 1997
The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery diseaseP Ferraresi, G Marchetti, C Legnani, et al.
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